Bulk Manufacturer of Controlled Substances Application: VICI Health Sciences, LLC, 46185 [2023-15279]

Download as PDF 46185 Federal Register / Vol. 88, No. 137 / Wednesday, July 19, 2023 / Notices service for any party/parties without a method of electronic service noted on the attached Certificate of Service and shall file proof of service on the Electronic Document Information System (EDIS). The Commission vote for this determination took place on July 13, 2023. The authority for the Commission’s determination is contained in section 337 of the Tariff Act of 1930, as amended (19 U.S.C. 1337), and in part 210 of the Commission’s Rules of Practice and Procedure (19 CFR part 210). By order of the Commission. Issued: July 13, 2023. Lisa Barton, Secretary to the Commission. [FR Doc. 2023–15235 Filed 7–18–23; 8:45 am] BILLING CODE 7020–02–P DEPARTMENT OF JUSTICE [Docket No. DEA–1230] Bulk Manufacturer of Controlled Substances Application: VICI Health Sciences, LLC Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: VICI Health Sciences, LLC has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information. DATES: Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may submit electronic comments on or objections to the issuance of the proposed registration on or before September 18, 2023. Such persons may also file a written request for a hearing on the application on or before September 18, 2023. ADDRESSES: The Drug Enforcement Administration requires that all SUMMARY: comments be submitted electronically through the Federal eRulemaking Portal, which provides the ability to type short comments directly into the comment field on the web page or attach a file for lengthier comments. Please go to https://www.regulations.gov and follow the online instructions at that site for submitting comments. Upon submission of your comment, you will receive a Comment Tracking Number. Please be aware that submitted comments are not instantaneously available for public view on https://www.regulations.gov. If you have received a Comment Tracking Number, your comment has been successfully submitted and there is no need to resubmit the same comment. In accordance with 21 CFR 1301.33(a), this is notice that on May 12, 2023, VICI Health Sciences, LLC, 6655 Amberton Drive, Suite O, Elkridge, Maryland 21075, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): SUPPLEMENTARY INFORMATION: Controlled substance Drug code Ibogaine ........................................................................................................................................................................... Fentanyl related-compounds as defined in 21 CFR 1308.11(h) ..................................................................................... The company plans to bulk manufacture the listed controlled substances or their intermediates for sale to its customers. No other activities for these drug codes are authorized for this registration. Claude Redd, Acting Deputy Assistant Administrator. [FR Doc. 2023–15279 Filed 7–18–23; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE ddrumheller on DSK120RN23PROD with NOTICES1 Notice of Lodging of Proposed Second Amendment to Consent Decree Under CERCLA On July 12, 2023, the Department of Justice lodged a proposed Second Amendment To Consent Decree with the United States District Court for the Northern District of New York in the lawsuit entitled United States of America v. Boise Cascade Corporation, et al., Civil Case No. 97–cv–1704 (TJM). The proposed Second Amendment To Consent Decree is intended to modify the Consent Decree entered by the Court on February 20, 1998, as amended by the First Amendment To Consent Decree, entered by the Court on June 7, 2005. The Complaint in this matter was filed on November 20, 1997. Under the VerDate Sep<11>2014 00:36 Jul 19, 2023 Jkt 259001 Consent Decree, as amended in 2005, Settling Defendants are required to perform remedial work at the Sealand Superfund Restoration Site (‘‘the Site’’) located in Lisbon, New York and to reimburse the Environmental Protection Agency’s response costs pertaining to this Site in accordance with the requirements of the Comprehensive Environmental Response, Compensation and Liability Act (‘‘CERCLA’’), 42 U.S.C. 9601–9675. One of the Settling Defendants, SBC Holdings Inc. (‘‘SBC’’), now lacks the financial capability to continue these obligations. The proposed Second Amendment To Consent Decree includes an ability-topay-cash-out settlement with SBC in which it will pay $150,000 and removes SBC as a Settling Defendant responsible for future work and costs at the Site. The remaining Settling Defendants have agreed to the proposed Second Amendment and will continue to be jointly and severally liable for all work and costs at the Site. The publication of this notice opens a period for public comment on the Consent Decree. Comments should be addressed to the Assistant Attorney General, Environment and Natural Resources Division, and should refer to United States of America v. Boise Cascade Corporation, et al., Civil Case PO 00000 Frm 00059 Fmt 4703 Sfmt 4703 7260 9850 Schedule I I No. 97–cv–1704 (TJM), D.J. Ref. No. 90– 11–3–1144/1. All comments must be submitted no later than thirty (30) days after the publication date of this notice. Comments may be submitted either by email or by mail: To submit comments: Send them to: By email ....... pubcomment-ees.enrd@ usdoj.gov. Assistant Attorney General, U.S. DOJ—ENRD, P.O. Box 7611, Washington, DC 20044–7611. By mail ......... During the public comment period, the Consent Decree may be examined and downloaded at this Justice Department website: https:// www.justice.gov/enrd/consent-decrees. We will provide a paper copy of the Consent Decree upon written request and payment of reproduction costs. Please mail your request for a paper copy and payment to: Consent Decree Library, U.S. DOJ—ENRD, P.O. Box 7611, Washington, DC 20044–7611. Please enclose a check or money order for $5.75 (25 cents per page E:\FR\FM\19JYN1.SGM 19JYN1

Agencies

[Federal Register Volume 88, Number 137 (Wednesday, July 19, 2023)]
[Notices]
[Page 46185]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-15279]


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DEPARTMENT OF JUSTICE

[Docket No. DEA-1230]


Bulk Manufacturer of Controlled Substances Application: VICI 
Health Sciences, LLC

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: VICI Health Sciences, LLC has applied to be registered as a 
bulk manufacturer of basic class(es) of controlled substance(s). Refer 
to SUPPLEMENTARY INFORMATION listed below for further drug information.

DATES: Registered bulk manufacturers of the affected basic class(es), 
and applicants therefore, may submit electronic comments on or 
objections to the issuance of the proposed registration on or before 
September 18, 2023. Such persons may also file a written request for a 
hearing on the application on or before September 18, 2023.

ADDRESSES: The Drug Enforcement Administration requires that all 
comments be submitted electronically through the Federal eRulemaking 
Portal, which provides the ability to type short comments directly into 
the comment field on the web page or attach a file for lengthier 
comments. Please go to https://www.regulations.gov and follow the 
online instructions at that site for submitting comments. Upon 
submission of your comment, you will receive a Comment Tracking Number. 
Please be aware that submitted comments are not instantaneously 
available for public view on https://www.regulations.gov. If you have 
received a Comment Tracking Number, your comment has been successfully 
submitted and there is no need to resubmit the same comment.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this 
is notice that on May 12, 2023, VICI Health Sciences, LLC, 6655 
Amberton Drive, Suite O, Elkridge, Maryland 21075, applied to be 
registered as a bulk manufacturer of the following basic class(es) of 
controlled substance(s):

------------------------------------------------------------------------
        Controlled substance            Drug code          Schedule
------------------------------------------------------------------------
Ibogaine...........................            7260  I
Fentanyl related-compounds as                  9850  I
 defined in 21 CFR 1308.11(h).
------------------------------------------------------------------------

    The company plans to bulk manufacture the listed controlled 
substances or their intermediates for sale to its customers. No other 
activities for these drug codes are authorized for this registration.

Claude Redd,
Acting Deputy Assistant Administrator.
[FR Doc. 2023-15279 Filed 7-18-23; 8:45 am]
BILLING CODE P
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